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FGF21 deficiency is associated with childhood obesity, insulin resistance and hypoadiponectinaemia: The BCAMS Study
1Department of Endocrinology, Key Laboratory of Endocrinology, Ministry of Health, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College (CAMS & PUMC), Beijing 100730, China.
Insights
Fibroblast growth factor 21 (FGF21) levels were lower in obese children and linked to insulin resistance. FGF21 deficiency, not resistance, may cause metabolic issues in youth.
Area of Science:
- Endocrinology
- Metabolic Health
- Paediatric Research
Background:
- Fibroblast growth factor 21 (FGF21) influences metabolic homeostasis.
- Circulating FGF21 is linked to metabolic disorders in adults.
- Paediatric data on FGF21 and metabolic health is limited.
Purpose of the Study:
- Investigate FGF21 levels in relation to obesity, insulin resistance (IR), and metabolic syndrome (MetS) in children.
- Examine the association between FGF21 and adipokines (adiponectin, leptin, resistin) in a paediatric cohort.
- Clarify the role of FGF21 in paediatric metabolic health.
Main Methods:
- Cross-sectional study of 3231 Chinese children aged 6-18.
- Measured serum FGF21, insulin, HOMA-IR, adipokines, and anthropometric data.
- Statistical analyses included regression and odds ratio calculations.
Main Results:
- FGF21 levels showed gender and puberty-related variations.
- Obese children had lower FGF21 levels, negatively correlated with insulin, HOMA-IR, and leptin.
- Lower FGF21 quintiles were associated with increased odds of IR and MetS.
- Resistin positively predicted FGF21, while FGF21 positively predicted adiponectin.
Conclusions:
- FGF21 associations with obesity, IR, and MetS in children are inverse to adult findings.
- FGF21 deficiency, rather than resistance, may contribute to IR and hypoadiponectinemia in youth.
- Findings suggest a distinct role for FGF21 in paediatric metabolic regulation.
Objective:
Fibroblast growth factor 21 (FGF21) exerts beneficial effects on metabolic homoeostasis and has been reported to be regulated by adiponectin, leptin and resistin. However, while an association between increased circulating FGF21 and metabolic disorders has been reported in adults, paediatric-specific data are lacking.
Design And Methods:
This study investigated the relationship between FGF21 levels and obesity, insulin resistance (IR), the metabolic syndrome (MetS) and adipokines (adiponectin, leptin and resistin) in a cohort of 3231 Chinese youngsters aged 6-18.
Results:
There were gender- and puberty-related differences in FGF21 levels. Unexpectedly, FGF21 levels were decreased in children with obesity, and negatively correlated with insulin, HOMA-IR and leptin levels after adjusting for age, gender, puberty and lifestyle factors. Moreover, multiple regression analyses showed that serum FGF21 positively predicted adiponectin levels while resistin positively predicted FGF21 levels independent of BMI (P<0.05). Children in the lowest FGF21 quintile were more likely to have IR (OR: 1.85, 95% CI: 1.41-2.42; P=0.002) and MetS (OR: 1.62, 95% CI: 1.14-2.28; P=0.007) than those in the highest quintile. Further adjusting for BMI and/or the three adipokines modified the association of FGF21 with MetS (P>0.10) but not with IR (P<0.01).
Conclusion:
Although the associations between adiponectin, leptin, resistin and metabolic abnormalities in our paediatric population were similar to those in adults, correlations of FGF21 levels with obesity, IR and MetS were the inverse of those found in adults. Our present findings suggest that FGF21 deficiency, rather than resistance, contribute to IR and hypoadiponectinaemia independently of obesity in young people.
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